Canonical Allele Identifier: CA347714268
Gene: CNNM4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.97427278C>A (hg19) chr2:g.96761541C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96761541C>A , CM000664.2:g.96761541C>A GRCh38
NC_000002.11:g.97427278C>A , CM000664.1:g.97427278C>A GRCh37
NC_000002.10:g.96791005C>A NCBI36
NG_016608.1:g.5640C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377075.3:c.542C>A MANE Select ENSP00000366275.2:p.Pro181His
ENST00000377075.2:c.542C>A ENSP00000366275.2:p.Pro181His
NM_020184.3:c.542C>A NP_064569.3:p.Pro181His
XM_005263914.2:c.542C>A XP_005263971.1:p.Pro181His
XM_005263915.2:c.542C>A XP_005263972.1:p.Pro181His
XM_011510955.1:c.542C>A XP_011509257.1:p.Pro181His
XM_011510956.1:c.542C>A XP_011509258.1:p.Pro181His
XM_005263914.4:c.542C>A XP_005263971.1:p.Pro181His
XM_005263915.4:c.542C>A XP_005263972.1:p.Pro181His
XM_011510955.3:c.542C>A XP_011509257.1:p.Pro181His
XM_011510956.3:c.542C>A XP_011509258.1:p.Pro181His
NM_020184.4:c.542C>A MANE Select NP_064569.3:p.Pro181His
Search 100 bp 5'
Search 100 bp 3'